Futibatinib
Records for this ingredient, by country (identity only).
ATC L01EN04 · 9 markets · 12 records
AU 3 records · 1 shown of 1
- 4 mgtabletLYTGOBILYTGOBI futibatinib 4 mg tablet blister pack
1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商
Full list in the data package Lista completa en el paquete de datos 完整清单见数据包 完整清單見資料包
GB 1 records · 1 shown of 1
- 4 mgtabletLYTGOBI
SG 1 records · 1 shown of 1
- 4 mgtabletLYTGOBI
ES 1 records · 1 shown of 1
- 4 mgtabletLYTGOBI
HK 1 records · 0 shown of 0
1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商
Full list in the data package Lista completa en el paquete de datos 完整清单见数据包 完整清單見資料包
JP 1 records · 1 shown of 1
- 4 mgtabletリトゴビ錠4mg
EU 1 records · 0 shown of 0
EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.
1 records · 0 manufacturers 1 registros · 0 fabricantes 1 个记录 · 0 个厂家 1 個記錄 · 0 個廠商
Full list in the data package Lista completa en el paquete de datos 完整清单见数据包 完整清單見資料包
FR 1 records · 1 shown of 1
- 4 mgtabletLYTGOBI 4 mg, comprimé pelliculé
| Strength / form / release | US | GB | AU | SG | ES | HK | JP | EU | FR |
|---|---|---|---|---|---|---|---|---|---|
| 4 mg tablet | LYTGOBI | LYTGOBI | LYTGOBI LYTGOBI futibatinib 4 mg tablet blister pack | LYTGOBI | LYTGOBI | リトゴビ錠4mg | LYTGOBI 4 mg, comprimé pelliculé | ||
| 16 mg tablet | LYTGOBI | ||||||||
unknown | LYTGOBI | LYTGOBI | LYTGOBI |
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Each country column shows the locally registered trade names — not translations.
“not disclosed” means the source does not publish the strength — it does not mean the product has none.
Hong Kong records are name/ingredient-level only: no strength, dosage form or registration status; on the register does not prove current supply.
Australia ARTG data has no registration-status column, so status is shown as unknown; being on the register does not mean currently marketed.
EU centralised authorisation (EMA) — Authorised at EU level — not a record of sale in any single country. The EU register carries no strength, dosage form or pack size.
Discontinued, withdrawn or unverified-status products are hidden by default; Hong Kong and Australia records are shown as exceptions.